FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection
PMA: P230009
·
Supplement: S002
·
Decision Oct 18, 2024
Classifications
1
FEI Numbers
11
Registration Numbers
11
Basic Information
- Device Name
- System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection
- Trade Name
- Shield
- PMA Number
- P230009
- Supplement Number
- S002
- Device Class
- FDA Class 3
- Product Code
- PHP
- Generic Name
- System, colorectal neoplasia, DNA methylation and hemoglobin detection
- Medical Specialty
- Unknown
- Advisory Committee
- Medical Genetics
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- October 18, 2024
- Date Received
- September 20, 2024
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Addition of a reagent storage and distribution facility
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| PHP | System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection | FDA class 3 | Unknown |